The Sickle Cell Disease Association of America Inc., a national nonprofit membership organization that advocates for people affected by sickle cell disease, will hold the Warrior Walkathon on Saturday, July 18, from 9 a.m. to noon at Lake Montebello in Baltimore.

“SCDAA is excited to host our 13th annual walkathon, again in Baltimore,” said Regina Hartfield, president and CEO of the association. “It’s a great opportunity to make a difference. Join us to raise vital funds in support of a universal cure. Walk alongside sickle cell warriors, caregivers, families, friends, community organizations, sororities, fraternities, industry leaders and supporters of the sickle cell community.”

For over a decade, the annual walkathon — formerly named Walk with the Stars — has raised more than $500,000 to support improvements in the quality of health, life and services for individuals, families and communities affected by sickle cell disease.

The Warrior Walkathon will begin with a warmup followed by the walk and awards ceremony. Participants can create and promote personal fundraising webpages to raise money for the Sickle Cell Disease Association of America Inc. and those affected by sickle cell disease.

The walkathon is free to attend, but registration is required. Participants who raise over $25 receive a T-shirt. To learn more and register, visit bit.ly/SCDAAWalk2026.

Sickle cell disease is a rare inherited blood disease causing red blood cells to take a sickle shape, which leads to blockages that prevent blood from reaching parts of the body. As a result, people with sickle cell complications can experience anemia, jaundice, gallstones, stroke, chronic pain, organ damage and premature death. More than 100,000 Americans live with sickle cell disease, and 2 million Americans have sickle cell trait. No universal cure exists.

Sickle Cell Disease Association of America Inc. advocates for people affected by sickle cell conditions and empowers community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure. The association and more than 50 member organizations support sickle cell research, public and professional health education and patient and community services. (sicklecelldisease.org)